304 related articles for article (PubMed ID: 28852778)
1. Pathogenic mutation in the ALS/FTD gene, CCNF, causes elevated Lys48-linked ubiquitylation and defective autophagy.
Lee A; Rayner SL; Gwee SSL; De Luca A; Shahheydari H; Sundaramoorthy V; Ragagnin A; Morsch M; Radford R; Galper J; Freckleton S; Shi B; Walker AK; Don EK; Cole NJ; Yang S; Williams KL; Yerbury JJ; Blair IP; Atkin JD; Molloy MP; Chung RS
Cell Mol Life Sci; 2018 Jan; 75(2):335-354. PubMed ID: 28852778
[TBL] [Abstract][Full Text] [Related]
2. The E3 Ubiquitin Ligase SCF Cyclin F Promotes Sequestosome-1/p62 Insolubility and Foci Formation and is Dysregulated in ALS and FTD Pathogenesis.
Davidson JM; Wu SSL; Rayner SL; Cheng F; Duncan K; Russo C; Newbery M; Ding K; Scherer NM; Balez R; García-Redondo A; Rábano A; Rosa-Fernandes L; Ooi L; Williams KL; Morsch M; Blair IP; Di Ieva A; Yang S; Chung RS; Lee A
Mol Neurobiol; 2023 Sep; 60(9):5034-5054. PubMed ID: 37243816
[TBL] [Abstract][Full Text] [Related]
3. TDP-43 is a ubiquitylation substrate of the SCF
Rayner SL; Yang S; Farrawell NE; Jagaraj CJ; Cheng F; Davidson JM; Luu L; Redondo AG; Rábano A; Borrego-Hernández D; Atkin JD; Morsch M; Blair IP; Yerbury JJ; Chung R; Lee A
Neurobiol Dis; 2022 Jun; 167():105673. PubMed ID: 35231559
[TBL] [Abstract][Full Text] [Related]
4. Casein kinase II phosphorylation of cyclin F at serine 621 regulates the Lys48-ubiquitylation E3 ligase activity of the SCF
Lee A; Rayner SL; De Luca A; Gwee SSL; Morsch M; Sundaramoorthy V; Shahheydari H; Ragagnin A; Shi B; Yang S; Williams KL; Don EK; Walker AK; Zhang KY; Yerbury JJ; Cole NJ; Atkin JD; Blair IP; Molloy MP; Chung RS
Open Biol; 2017 Oct; 7(10):. PubMed ID: 29021214
[TBL] [Abstract][Full Text] [Related]
5. ALS/FTD-causing mutation in cyclin F causes the dysregulation of SFPQ.
Rayner SL; Cheng F; Hogan AL; Grima N; Yang S; Ke YD; Au CG; Morsch M; De Luca A; Davidson JM; Molloy MP; Shi B; Ittner LM; Blair I; Chung RS; Lee A
Hum Mol Genet; 2021 May; 30(11):971-984. PubMed ID: 33729478
[TBL] [Abstract][Full Text] [Related]
6. TDP-43 pathology and functional deficits in wild-type and ALS/FTD mutant cyclin F mouse models.
van Hummel A; Sabale M; Przybyla M; van der Hoven J; Chan G; Feiten AF; Chung RS; Ittner LM; Ke YD
Neuropathol Appl Neurobiol; 2023 Apr; 49(2):e12902. PubMed ID: 36951214
[TBL] [Abstract][Full Text] [Related]
7. CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.
Williams KL; Topp S; Yang S; Smith B; Fifita JA; Warraich ST; Zhang KY; Farrawell N; Vance C; Hu X; Chesi A; Leblond CS; Lee A; Rayner SL; Sundaramoorthy V; Dobson-Stone C; Molloy MP; van Blitterswijk M; Dickson DW; Petersen RC; Graff-Radford NR; Boeve BF; Murray ME; Pottier C; Don E; Winnick C; McCann EP; Hogan A; Daoud H; Levert A; Dion PA; Mitsui J; Ishiura H; Takahashi Y; Goto J; Kost J; Gellera C; Gkazi AS; Miller J; Stockton J; Brooks WS; Boundy K; Polak M; Muñoz-Blanco JL; Esteban-Pérez J; Rábano A; Hardiman O; Morrison KE; Ticozzi N; Silani V; de Belleroche J; Glass JD; Kwok JB; Guillemin GJ; Chung RS; Tsuji S; Brown RH; García-Redondo A; Rademakers R; Landers JE; Gitler AD; Rouleau GA; Cole NJ; Yerbury JJ; Atkin JD; Shaw CE; Nicholson GA; Blair IP
Nat Commun; 2016 Apr; 7():11253. PubMed ID: 27080313
[TBL] [Abstract][Full Text] [Related]
8. Cyclin F, Neurodegeneration, and the Pathogenesis of ALS/FTD.
Rayner SL; Hogan A; Davidson JM; Cheng F; Luu L; Morsch M; Blair I; Chung R; Lee A
Neuroscientist; 2024 Apr; 30(2):214-228. PubMed ID: 36062310
[TBL] [Abstract][Full Text] [Related]
9. ALS-linked CCNF variant disrupts motor neuron ubiquitin homeostasis.
Farrawell NE; Bax M; McAlary L; McKenna J; Maksour S; Do-Ha D; Rayner SL; Blair IP; Chung RS; Yerbury JJ; Ooi L; Saunders DN
Hum Mol Genet; 2023 Jul; 32(14):2386-2398. PubMed ID: 37220877
[TBL] [Abstract][Full Text] [Related]
10. C9orf72 ALS-FTD: recent evidence for dysregulation of the autophagy-lysosome pathway at multiple levels.
Beckers J; Tharkeshwar AK; Van Damme P
Autophagy; 2021 Nov; 17(11):3306-3322. PubMed ID: 33632058
[TBL] [Abstract][Full Text] [Related]
11. ALS/FTD-associated mutation in cyclin F inhibits ER-Golgi trafficking, inducing ER stress, ERAD and Golgi fragmentation.
Ragagnin AMG; Sundaramoorthy V; Farzana F; Gautam S; Saravanabavan S; Takalloo Z; Mehta P; Do-Ha D; Parakh S; Shadfar S; Hunter J; Vidal M; Jagaraj CJ; Brocardo M; Konopka A; Yang S; Rayner SL; Williams KL; Blair IP; Chung RS; Lee A; Ooi L; Atkin JD
Sci Rep; 2023 Nov; 13(1):20467. PubMed ID: 37993492
[TBL] [Abstract][Full Text] [Related]
12. Expression of ALS/FTD-linked mutant CCNF in zebrafish leads to increased cell death in the spinal cord and an aberrant motor phenotype.
Hogan AL; Don EK; Rayner SL; Lee A; Laird AS; Watchon M; Winnick C; Tarr IS; Morsch M; Fifita JA; Gwee SSL; Formella I; Hortle E; Yuan KC; Molloy MP; Williams KL; Nicholson GA; Chung RS; Blair IP; Cole NJ
Hum Mol Genet; 2017 Jul; 26(14):2616-2626. PubMed ID: 28444311
[TBL] [Abstract][Full Text] [Related]
13. Mutations of CCNF gene is rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia from Mainland China.
Pan C; Jiao B; Xiao T; Hou L; Zhang W; Liu X; Xu J; Tang B; Shen L
Amyotroph Lateral Scler Frontotemporal Degener; 2017 May; 18(3-4):265-268. PubMed ID: 28281833
[TBL] [Abstract][Full Text] [Related]
14. Investigating CCNF mutations in a Taiwanese cohort with amyotrophic lateral sclerosis.
Tsai PC; Liao YC; Chen PL; Guo YC; Chen YH; Jih KY; Lin KP; Soong BW; Tsai CP; Lee YC
Neurobiol Aging; 2018 Feb; 62():243.e1-243.e6. PubMed ID: 29102476
[TBL] [Abstract][Full Text] [Related]
15. Pathogenic mutations in the ALS gene CCNF cause cytoplasmic mislocalization of Cyclin F and elevated VCP ATPase activity.
Yu Y; Nakagawa T; Morohoshi A; Nakagawa M; Ishida N; Suzuki N; Aoki M; Nakayama K
Hum Mol Genet; 2019 Oct; 28(20):3486-3497. PubMed ID: 31577344
[TBL] [Abstract][Full Text] [Related]
16. SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis.
Le Ber I; Camuzat A; Guerreiro R; Bouya-Ahmed K; Bras J; Nicolas G; Gabelle A; Didic M; De Septenville A; Millecamps S; Lenglet T; Latouche M; Kabashi E; Campion D; Hannequin D; Hardy J; Brice A;
JAMA Neurol; 2013 Nov; 70(11):1403-10. PubMed ID: 24042580
[TBL] [Abstract][Full Text] [Related]
17. The converging roles of sequestosome-1/p62 in the molecular pathways of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD).
Davidson JM; Chung RS; Lee A
Neurobiol Dis; 2022 May; 166():105653. PubMed ID: 35143965
[TBL] [Abstract][Full Text] [Related]
18. Genetic and Phenotypic Spectrum of Amyotrophic Lateral Sclerosis Patients with CCNF Variants from a Large Chinese Cohort.
Zhao B; Jiang Q; Lin J; Wei Q; Li C; Hou Y; Cao B; Zhang L; Ou R; Liu K; Yang T; Xiao Y; Huang R; Shang H
Mol Neurobiol; 2023 Jul; 60(7):4150-4160. PubMed ID: 37171577
[TBL] [Abstract][Full Text] [Related]
19. Unbiased Label-Free Quantitative Proteomics of Cells Expressing Amyotrophic Lateral Sclerosis (ALS) Mutations in
Cheng F; De Luca A; Hogan AL; Rayner SL; Davidson JM; Watchon M; Stevens CH; Muñoz SS; Ooi L; Yerbury JJ; Don EK; Fifita JA; Villalva MD; Suddull H; Chapman TR; Hedl TJ; Walker AK; Yang S; Morsch M; Shi B; Blair IP; Laird AS; Chung RS; Lee A
Front Mol Neurosci; 2021; 14():627740. PubMed ID: 33986643
[TBL] [Abstract][Full Text] [Related]
20. SQSTM1 variant in disorders of the frontotemporal dementia-amyotrophic lateral sclerosis spectrum: identification of a novel heterozygous variant and a review of the literature.
Li W; Gao H; Dong X; Zheng D
J Neurol; 2021 Apr; 268(4):1351-1357. PubMed ID: 33125541
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
